nsv3919076
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37, GRCh38, NCBI36
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:10,642,632
- Description:GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3 AND See cases
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 47311 SVs from 129 studies. See in: genome view
Overlapping variant regions from other studies: 45209 SVs from 130 studies. See in: genome view
Overlapping variant regions from other studies: 11391 SVs from 37 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nsv3919076 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000019.10 | Chr19 | 47,929,575 | 58,572,206 |
| nsv3919076 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000019.9 | Chr19 | 48,432,832 | 59,083,573 |
| nsv3919076 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000019.8 | Chr19 | 53,124,644 | 63,775,385 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15145773 | copy number gain | Multiple | Multiple | See cases | Pathogenic | ClinVar | RCV000052915.6, VCV000059117.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nssv15145773 | Submitted genomic | NC_000019.10:g.(?_ 47929575)_(5857220 6_?)dup | GRCh38 (hg38) | NC_000019.10 | Chr19 | 47,929,575 | 58,572,206 |
| nssv15145773 | Submitted genomic | NC_000019.9:g.(?_4 8432832)_(59083573 _?)dup | GRCh37 (hg19) | NC_000019.9 | Chr19 | 48,432,832 | 59,083,573 |
| nssv15145773 | Submitted genomic | NC_000019.8:g.(?_5 3124644)_(63775385 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 53,124,644 | 63,775,385 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | HGVS | Type | Allele Origin | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15145773 | GRCh37: NC_000019.9:g.(?_48432832)_(59083573_?)dup, GRCh38: NC_000019.10:g.(?_47929575)_(58572206_?)dup, NCBI36: NC_000019.8:g.(?_53124644)_(63775385_?)dup | copy number gain | not provided | See cases | Pathogenic | ClinVar | RCV000052915.6, VCV000059117.1 | 3 |